KR0142424B1 - 베타-페녹시니트릴 화합물 - Google Patents
베타-페녹시니트릴 화합물Info
- Publication number
- KR0142424B1 KR0142424B1 KR1019890004018A KR890004018A KR0142424B1 KR 0142424 B1 KR0142424 B1 KR 0142424B1 KR 1019890004018 A KR1019890004018 A KR 1019890004018A KR 890004018 A KR890004018 A KR 890004018A KR 0142424 B1 KR0142424 B1 KR 0142424B1
- Authority
- KR
- South Korea
- Prior art keywords
- group
- compound
- formula
- alkyl
- optionally substituted
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 86
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 34
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 18
- 125000005843 halogen group Chemical group 0.000 claims abstract description 14
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 13
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 11
- 125000003118 aryl group Chemical group 0.000 claims abstract description 10
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 9
- 150000002367 halogens Chemical class 0.000 claims abstract description 9
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 5
- 125000001424 substituent group Chemical group 0.000 claims abstract description 5
- 230000000855 fungicidal effect Effects 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 46
- 238000000034 method Methods 0.000 claims description 18
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 17
- -1 or cyan No Chemical group 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 11
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 11
- 125000002947 alkylene group Chemical group 0.000 claims description 10
- 230000000844 anti-bacterial effect Effects 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 10
- 239000004094 surface-active agent Substances 0.000 claims description 8
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 7
- 239000002585 base Substances 0.000 claims description 6
- 239000000417 fungicide Substances 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000003880 polar aprotic solvent Substances 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 125000004423 acyloxy group Chemical group 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 claims description 4
- 125000004995 haloalkylthio group Chemical group 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 229910052727 yttrium Inorganic materials 0.000 claims description 4
- 208000031888 Mycoses Diseases 0.000 claims description 3
- 229910000102 alkali metal hydride Inorganic materials 0.000 claims description 3
- 150000008046 alkali metal hydrides Chemical class 0.000 claims description 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 4
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000003586 protic polar solvent Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 abstract description 8
- 239000000460 chlorine Substances 0.000 abstract description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract description 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract description 5
- 229910052794 bromium Inorganic materials 0.000 abstract description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 5
- 125000004438 haloalkoxy group Chemical group 0.000 abstract description 4
- 125000001188 haloalkyl group Chemical group 0.000 abstract description 4
- 229910052731 fluorine Inorganic materials 0.000 abstract description 3
- 239000011737 fluorine Substances 0.000 abstract description 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000000746 allylic group Chemical group 0.000 abstract 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 23
- 241000196324 Embryophyta Species 0.000 description 22
- 239000013543 active substance Substances 0.000 description 19
- 241000233866 Fungi Species 0.000 description 18
- 239000000843 powder Substances 0.000 description 18
- 238000012360 testing method Methods 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 239000007921 spray Substances 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 201000010099 disease Diseases 0.000 description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 238000011282 treatment Methods 0.000 description 9
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 8
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 8
- 239000011149 active material Substances 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 235000013339 cereals Nutrition 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 239000007900 aqueous suspension Substances 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 238000005507 spraying Methods 0.000 description 6
- 241000123650 Botrytis cinerea Species 0.000 description 5
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000004495 emulsifiable concentrate Substances 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- XADQMQWAUWCAJS-UHFFFAOYSA-N 2-(bromomethyl)-2-pyridin-3-ylbutanenitrile Chemical compound CCC(CBr)(C#N)C1=CC=CN=C1 XADQMQWAUWCAJS-UHFFFAOYSA-N 0.000 description 4
- XMPUONNGCGZOFL-UHFFFAOYSA-N 4-(4-chlorophenoxy)-2-pyridin-3-ylbutanenitrile Chemical compound C1=CC(Cl)=CC=C1OCCC(C#N)C1=CC=CN=C1 XMPUONNGCGZOFL-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 241000209219 Hordeum Species 0.000 description 4
- 240000007594 Oryza sativa Species 0.000 description 4
- 235000007164 Oryza sativa Nutrition 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 230000002538 fungal effect Effects 0.000 description 4
- 230000012010 growth Effects 0.000 description 4
- 238000001727 in vivo Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 4
- 235000019341 magnesium sulphate Nutrition 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 230000008635 plant growth Effects 0.000 description 4
- 235000009566 rice Nutrition 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 4
- WJNPSUDTHFUFPJ-UHFFFAOYSA-N 4-(4-chlorophenoxy)-2-methyl-2-pyridin-3-ylbutanenitrile Chemical compound C=1C=CN=CC=1C(C)(C#N)CCOC1=CC=C(Cl)C=C1 WJNPSUDTHFUFPJ-UHFFFAOYSA-N 0.000 description 3
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 241000221785 Erysiphales Species 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 208000004770 Fusariosis Diseases 0.000 description 3
- 241000223218 Fusarium Species 0.000 description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 235000019270 ammonium chloride Nutrition 0.000 description 3
- 239000010779 crude oil Substances 0.000 description 3
- 235000021186 dishes Nutrition 0.000 description 3
- 239000003480 eluent Substances 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000012312 sodium hydride Substances 0.000 description 3
- 229910000104 sodium hydride Inorganic materials 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- 241000223600 Alternaria Species 0.000 description 2
- 241000228245 Aspergillus niger Species 0.000 description 2
- 241000221198 Basidiomycota Species 0.000 description 2
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000735576 Felicia Species 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- 241001555627 Melonis Species 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241001558929 Sclerotium <basidiomycota> Species 0.000 description 2
- 241001533598 Septoria Species 0.000 description 2
- 240000003768 Solanum lycopersicum Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 239000006013 carbendazim Substances 0.000 description 2
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
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- 238000011109 contamination Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- FJBFPHVGVWTDIP-UHFFFAOYSA-N dibromomethane Chemical compound BrCBr FJBFPHVGVWTDIP-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000006196 drop Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003889 eye drop Substances 0.000 description 2
- 229940012356 eye drops Drugs 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 230000000887 hydrating effect Effects 0.000 description 2
- 150000007529 inorganic bases Chemical class 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 150000007530 organic bases Chemical class 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical class OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 239000003444 phase transfer catalyst Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 2
- 229920000053 polysorbate 80 Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 230000035755 proliferation Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000004550 soluble concentrate Substances 0.000 description 2
- 238000003892 spreading Methods 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical class C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
- YYFLBDSMQRWARK-UHFFFAOYSA-N 1-(2-bromoethoxy)-4-chlorobenzene Chemical compound ClC1=CC=C(OCCBr)C=C1 YYFLBDSMQRWARK-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- XIDPTYGBMBAESA-UHFFFAOYSA-N 2-[(2,4-dibromophenoxy)methyl]-2-pyridin-3-ylbutanenitrile Chemical compound C=1C=CN=CC=1C(CC)(C#N)COC1=CC=C(Br)C=C1Br XIDPTYGBMBAESA-UHFFFAOYSA-N 0.000 description 1
- PIVCLJCBCXOKFB-UHFFFAOYSA-N 2-[(2,4-dichlorophenoxy)methyl]-2-pyridin-3-ylbutanenitrile Chemical compound C=1C=CN=CC=1C(CC)(C#N)COC1=CC=C(Cl)C=C1Cl PIVCLJCBCXOKFB-UHFFFAOYSA-N 0.000 description 1
- JDAKNCPKASDNDC-UHFFFAOYSA-N 2-[(3,4-dichlorophenoxy)methyl]-2-pyridin-3-yl-3-trimethylsilylpropanenitrile Chemical compound C=1C=CN=CC=1C(C[Si](C)(C)C)(C#N)COC1=CC=C(Cl)C(Cl)=C1 JDAKNCPKASDNDC-UHFFFAOYSA-N 0.000 description 1
- ZTWVSUUDBPCDJU-UHFFFAOYSA-N 2-[(3,4-dichlorophenoxy)methyl]-2-pyridin-3-ylbutanenitrile Chemical compound C=1C=CN=CC=1C(CC)(C#N)COC1=CC=C(Cl)C(Cl)=C1 ZTWVSUUDBPCDJU-UHFFFAOYSA-N 0.000 description 1
- XUCSUPRFGYXFLT-UHFFFAOYSA-N 2-[(3,4-dichlorophenoxy)methyl]-2-pyridin-3-ylpentanenitrile Chemical compound C=1C=CN=CC=1C(CCC)(C#N)COC1=CC=C(Cl)C(Cl)=C1 XUCSUPRFGYXFLT-UHFFFAOYSA-N 0.000 description 1
- LTJNQNPENKBMRV-UHFFFAOYSA-N 2-[(3,4-dichlorophenyl)sulfanylmethyl]-2-pyridin-3-ylbutanenitrile Chemical compound N1=CC(=CC=C1)C(C#N)(CSC1=CC(=C(C=C1)Cl)Cl)CC LTJNQNPENKBMRV-UHFFFAOYSA-N 0.000 description 1
- XPAHBULEWRSGPM-UHFFFAOYSA-N 2-[(3,5-dichlorophenoxy)methyl]-2-pyridin-3-ylbutanenitrile Chemical compound C=1C=CN=CC=1C(CC)(C#N)COC1=CC(Cl)=CC(Cl)=C1 XPAHBULEWRSGPM-UHFFFAOYSA-N 0.000 description 1
- XVUCTKAHZYAWOC-UHFFFAOYSA-N 2-[(4-bromophenoxy)methyl]-2-pyridin-3-ylbutanenitrile Chemical compound C=1C=CN=CC=1C(CC)(C#N)COC1=CC=C(Br)C=C1 XVUCTKAHZYAWOC-UHFFFAOYSA-N 0.000 description 1
- KSUHCRAMQTUZOF-UHFFFAOYSA-N 2-[(4-bromophenoxy)methyl]-4-pyridin-3-ylpentanenitrile Chemical compound C=1C=CN=CC=1C(C)CC(C#N)COC1=CC=C(Br)C=C1 KSUHCRAMQTUZOF-UHFFFAOYSA-N 0.000 description 1
- OGVHYPQLAHUARE-UHFFFAOYSA-N 2-[(4-bromophenyl)sulfanylmethyl]-2-pyridin-3-ylbutanenitrile Chemical compound N1=CC(=CC=C1)C(C#N)(CSC1=CC=C(C=C1)Br)CC OGVHYPQLAHUARE-UHFFFAOYSA-N 0.000 description 1
- LKGKYGOTNJFODE-UHFFFAOYSA-N 2-[(4-chlorophenoxy)methyl]-2-pyridin-3-yl-3-trimethylsilylpropanenitrile Chemical compound C=1C=CN=CC=1C(C[Si](C)(C)C)(C#N)COC1=CC=C(Cl)C=C1 LKGKYGOTNJFODE-UHFFFAOYSA-N 0.000 description 1
- OKRFRCKJZPZJJS-UHFFFAOYSA-N 2-[(4-chlorophenoxy)methyl]-2-pyridin-3-ylbutanenitrile Chemical compound C=1C=CN=CC=1C(CC)(C#N)COC1=CC=C(Cl)C=C1 OKRFRCKJZPZJJS-UHFFFAOYSA-N 0.000 description 1
- SEHKVQNOYMYRAC-UHFFFAOYSA-N 2-[(4-chlorophenoxy)methyl]-2-pyridin-3-ylpentanenitrile Chemical compound C=1C=CN=CC=1C(CCC)(C#N)COC1=CC=C(Cl)C=C1 SEHKVQNOYMYRAC-UHFFFAOYSA-N 0.000 description 1
- CVPQCPOSMNRJBS-UHFFFAOYSA-N 2-[(4-chlorophenyl)sulfanylmethyl]-2-pyridin-3-ylbutanenitrile Chemical compound N1=CC(=CC=C1)C(C#N)(CSC1=CC=C(C=C1)Cl)CC CVPQCPOSMNRJBS-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/57—Nitriles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Health & Medical Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Silicon Polymers (AREA)
- Materials For Photolithography (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8804411A FR2629455B1 (fr) | 1988-03-29 | 1988-03-29 | Derives de 2-(3-pyridinyl)3-(phenoxy) propanenitrile |
| FR88/04411 | 1988-03-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR890014481A KR890014481A (ko) | 1989-10-24 |
| KR0142424B1 true KR0142424B1 (ko) | 1998-06-01 |
Family
ID=9364924
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019890004018A KR0142424B1 (ko) | 1988-03-29 | 1989-03-29 | 베타-페녹시니트릴 화합물 |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US4999357A (de) |
| EP (1) | EP0335806B1 (de) |
| JP (1) | JP2752141B2 (de) |
| KR (1) | KR0142424B1 (de) |
| CN (1) | CN1026697C (de) |
| AT (1) | ATE129700T1 (de) |
| AU (1) | AU610709B2 (de) |
| BR (1) | BR8901569A (de) |
| CS (1) | CS274498B2 (de) |
| DD (1) | DD283608A5 (de) |
| DE (1) | DE68924662T2 (de) |
| DK (1) | DK172555B1 (de) |
| ES (1) | ES2081858T3 (de) |
| FI (1) | FI94628C (de) |
| FR (1) | FR2629455B1 (de) |
| GR (1) | GR3018900T3 (de) |
| HU (1) | HU207046B (de) |
| IE (1) | IE71019B1 (de) |
| IL (1) | IL89764A (de) |
| PL (1) | PL158210B1 (de) |
| PT (1) | PT90132B (de) |
| RU (1) | RU2094431C1 (de) |
| YU (1) | YU47478B (de) |
| ZA (1) | ZA892331B (de) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5180827A (en) * | 1988-03-29 | 1993-01-19 | Rhone-Poulenc Agrochimie | 2-(3-pyridyl) propanenitrile derivatives |
| US5266579A (en) * | 1989-05-05 | 1993-11-30 | Basf Aktiengesellschaft | Certain pyridine derivatives and the use thereof as fungicides |
| DE4018260A1 (de) * | 1990-06-07 | 1991-12-12 | Basf Ag | Derivate des (beta)-picolins und diese enthaltende pflanzenschutzmittel |
| JPH06225793A (ja) * | 1992-11-27 | 1994-08-16 | Nippon Kayaku Co Ltd | ６β，１４α−ジヒドロキシ−４−アンドロステン−３，１７−ジオンの新規製造法 |
| CA2253368A1 (en) * | 1996-04-02 | 1997-10-09 | Uniroyal Chemical Ltd./Ltee | Pyridylmethyl nitriles, amides and thioamides useful as fungicides |
| PL1701941T3 (pl) | 2003-12-11 | 2012-11-30 | Univ Texas | Związki przeznaczone do leczenia chorób, związanych z proliferacją komórek |
| PL2514742T3 (pl) * | 2006-03-31 | 2015-07-31 | Univ Texas | Leki przeciwnowotworowe będące pochodnymi kwasu kawowego dostępnymi biologicznie po podaniu doustnym |
| AU2009268841B2 (en) | 2008-07-08 | 2014-02-06 | Board Of Regents, The University Of Texas System | Novel inhibitors of proliferation and activation of signal transducer and activator of transcription (STATS) |
| KR101702464B1 (ko) | 2015-07-27 | 2017-02-06 | 충남대학교산학협력단 | 암 예방 및 치료용 조성물 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2555579B1 (fr) * | 1983-11-24 | 1987-11-20 | Rhone Poulenc Agrochimie | Nouveaux derives de pyridylacetonitriles, leur preparation et leur utilisation comme antifongiques dans le domaine agricole |
| US3397273A (en) * | 1966-02-18 | 1968-08-13 | Lilly Co Eli | Controlling phytopathogenic fungi on plants with 3-pyridyl methane derivatives |
| IE56045B1 (en) * | 1982-09-27 | 1991-03-27 | Shell Int Research | Fungicidally active compounds |
| DE3421179A1 (de) * | 1984-06-07 | 1985-12-12 | Basf Ag, 6700 Ludwigshafen | Azolylnitrile und diese enthaltende fungizide |
| DK383086A (da) * | 1985-08-21 | 1987-02-22 | Rohm & Haas | (2-cyano-2-arylethyl)pyridiner, deres fremstilling og deres anvendelse som fungicider |
| EP0311051A3 (de) * | 1987-10-06 | 1990-10-10 | SDS Biotech K.K. | Pyridylacetonitrilderivate |
-
1988
- 1988-03-29 FR FR8804411A patent/FR2629455B1/fr not_active Expired - Lifetime
-
1989
- 1989-03-20 US US07/326,004 patent/US4999357A/en not_active Expired - Fee Related
- 1989-03-23 DE DE68924662T patent/DE68924662T2/de not_active Expired - Fee Related
- 1989-03-23 EP EP89420103A patent/EP0335806B1/de not_active Expired - Lifetime
- 1989-03-23 AT AT89420103T patent/ATE129700T1/de not_active IP Right Cessation
- 1989-03-23 ES ES89420103T patent/ES2081858T3/es not_active Expired - Lifetime
- 1989-03-27 IL IL8976489A patent/IL89764A/en not_active IP Right Cessation
- 1989-03-28 CS CS185289A patent/CS274498B2/cs unknown
- 1989-03-28 PT PT90132A patent/PT90132B/pt not_active IP Right Cessation
- 1989-03-28 DD DD89326944A patent/DD283608A5/de not_active IP Right Cessation
- 1989-03-28 YU YU63589A patent/YU47478B/sh unknown
- 1989-03-28 HU HU891534A patent/HU207046B/hu not_active IP Right Cessation
- 1989-03-28 FI FI891476A patent/FI94628C/fi not_active IP Right Cessation
- 1989-03-28 RU SU894613893A patent/RU2094431C1/ru active
- 1989-03-28 AU AU31744/89A patent/AU610709B2/en not_active Ceased
- 1989-03-28 DK DK198901490A patent/DK172555B1/da not_active IP Right Cessation
- 1989-03-29 JP JP1077925A patent/JP2752141B2/ja not_active Expired - Lifetime
- 1989-03-29 KR KR1019890004018A patent/KR0142424B1/ko not_active IP Right Cessation
- 1989-03-29 IE IE98489A patent/IE71019B1/en not_active IP Right Cessation
- 1989-03-29 PL PL1989278529A patent/PL158210B1/pl unknown
- 1989-03-29 BR BR898901569A patent/BR8901569A/pt not_active IP Right Cessation
- 1989-03-29 CN CN89101940A patent/CN1026697C/zh not_active Expired - Fee Related
- 1989-03-29 ZA ZA892331A patent/ZA892331B/xx unknown
-
1996
- 1996-02-02 GR GR960400298T patent/GR3018900T3/el unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A201 | Request for examination | ||
| E902 | Notification of reason for refusal | ||
| E701 | Decision to grant or registration of patent right | ||
| GRNT | Written decision to grant | ||
| LAPS | Lapse due to unpaid annual fee |